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I7608

Sigma-Aldrich

4-Iodoanisole

98%

Synonym(s):

4-Iodophenyl methyl ether, 4-Methoxyiodobenzene

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About This Item

Linear Formula:
IC6H4OCH3
CAS Number:
696-62-8
Molecular Weight:
234.03
Beilstein:
1906692
EC Number:
211-798-7
MDL number:
MFCD00001056
UNSPSC Code:
12352100
PubChem Substance ID:
24896119
NACRES:
NA.22

Assay

98%

bp

237 °C/726 mmHg (lit.)

mp

50-53 °C (lit.)

SMILES string

COc1ccc(I)cc1

InChI

1S/C7H7IO/c1-9-7-4-2-6(8)3-5-7/h2-5H,1H3

InChI key

SYSZENVIJHPFNL-UHFFFAOYSA-N

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

233.6 °F - closed cup

Flash Point(C)

112 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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[Studies on the effect of 3 varieties of an anti-adhesive mineral oil izoform on the skin of mice].
J Rubisz-Brzezińska et al.
Przeglad dermatologiczny, 67(5), 573-580 (1980-09-01)
M Arivazhagan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 113, 236-249 (2013-06-04)
The solid phase FT-IR and FT-Raman spectra of P-iodoanisole (P-IA) have been recorded in the regions 400-4000 and 50-4000 cm(-1), respectively. The spectra were interpreted in terms of fundamentals modes, combination and overtone bands. The structure of the molecule was
George W Kabalka et al.
Nuclear medicine and biology, 29(8), 841-843 (2002-11-28)
Arylboronate esters are converted to iodine-123 labeled aryl iodides using no-carrier-added iodine-123 labeled sodium iodide in the presence of chloramine-T. High yields of radiochemically pure products are obtained.
P N Rizk et al.
Xenobiotica; the fate of foreign compounds in biological systems, 25(2), 143-150 (1995-02-01)
1. The oxidative metabolism of 4-iodoanisole (1) by liver microsomes from beta-naphthoflavone-treated rats yields 4-iodophenol (2) 2-iodo-5-methoxyphenol (3), 2-methoxy-5-iodophenol (4), 4-methoxyphenol (5), and 3-methoxyphenol (6) in relative yields of 5:2:4:1:1 respectively. 2. [3 5-2H2]-1 was converted to the same five

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